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CS-W001157 4
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(S)-2-((tert-Butoxycarbonyl)amino)-3-cyclopentylpropanoic acid

  • CAS No. 143415-31-0

  • Cat. No. CS-0011029
  • Purity≥97%
  • MDL No.MFCD03094885

*For research and further manufacturing use only, not for direct human use.

(S)-2-((tert-Butoxycarbonyl)amino)-3-cyclopentylpropanoic acid|CS-0011029

Structure of 143415-31-0

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General Information

  • CAS No. 143415-31-0
  • Cat. No. CS-0011029
  • Purity ≥97%
  • MDL No. MFCD03094885
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₃H₂₃NO₄
  • Molecular Weight 257.33
  • Synonym(s) Boc-L-CyClopentylalanine
  • SMILES O=C(O)[C@@H](NC(OC(C)(C)C)=O)CC1CCCC1

Description

This chiral building block features a protected amino group and a cyclopentyl-substituted aliphatic chain, enabling direct incorporation into peptide architectures. The tert-butoxycarbonyl (Boc) moiety provides stable protection under standard conditions, while the (S)-configuration ensures stereochemical fidelity in synthetic sequences.

Application

(S)-2-((tert-Butoxycarbonyl)amino)-3-cyclopentylpropanoic acid serves as a valuable chiral building block for the synthesis of peptidomimetics and bioactive heterocycles. The Boc-protected amine enables straightforward coupling reactions, while the cyclopentyl group imparts conformational rigidity beneficial in medicinal chemistry optimization. Bench-stable and compatible with standard peptide synthesis protocols, it facilitates efficient purification and functional group manipulation in multi-step sequences.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   75.63
  • LogP   2.5446
  • H_Acceptors   3
  • H_Donors   2
  • Rotatable_Bonds   4

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